Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1555440555
rs1555440555
1.000 15 92953386 missense variant T/C snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 12 2007 2017
dbSNP: rs1555445563
rs1555445563
1.000 15 93012354 missense variant G/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 12 2007 2017
dbSNP: rs1555445685
rs1555445685
1.000 15 93014770 frameshift variant CT/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 12 2007 2017